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Wanling Yang

Showing results (101-110 of 168) with videos related to

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Rheumatology (Oxford, England)|January 20, 2025
Distinct genetic risk loci between biopsy-proven renal and non-renal lupus: a 10-year longitudinal cohortShirley Cw Chan, Yao Lei, Desmond Yh Yap, et al.
NPJ Genomic Medicine|August 16, 2018
Exome sequencing for paediatric-onset diseases: impact of the extensive involvement of medical geneticists in the diagnostic odysseyChristopher Cy Mak, Gordon Kc Leung, Gary Tk Mok, et al.
Journal of Autoimmunity|August 3, 2016
Identification of the long noncoding RNA NEAT1 as a novel inflammatory regulator acting through MAPK pathway in human lupusFeifei Zhang, Lingling Wu, Jie Qian, et al.
Lupus Science & Medicine|March 8, 2024
Association of genetic variation on X chromosome with systemic lupus erythematosus in both Thai and Chinese populationsPattarin Tangtanatakul, Yao Lei, Krisana Jaiwan, et al.
Frontiers in Genetics|July 29, 2020
Independent Replication on Genome-Wide Association Study Signals Identifies <i>IRF3</i> as a Novel Locus for Systemic Lupus ErythematosusFeixia Zhang, Yong-Fei Wang, Yan Zhang, et al.
Human Molecular Genetics|February 21, 2020
Genome-wide assessment of genetic risk for systemic lupus erythematosus and disease severityLingyan Chen, Yong-Fei Wang, Lu Liu, et al.
Scientific Reports|November 3, 2016
Novel identified associations of RGS1 and RASGRP1 variants in IgA NephropathyXu-Jie Zhou, Swapan K Nath, Yuan-Yuan Qi, et al.
Arthritis Research & Therapy|May 5, 2018
Meta-analysis of GWAS on both Chinese and European populations identifies GPR173 as a novel X chromosome susceptibility gene for SLEHuoru Zhang, Yan Zhang, Yong-Fei Wang, et al.
Nucleic Acids Research|March 17, 2018
A novel transcript isoform of STING that sequesters cGAMP and dominantly inhibits innate nucleic acid sensingPei-Hui Wang, Sin-Yee Fung, Wei-Wei Gao, et al.
Molecular Autism|January 4, 2018
Identification of mutations in the PI3K-AKT-mTOR signalling pathway in patients with macrocephaly and developmental delay and/or autismKit San Yeung, Winnie Wan Yee Tso, Janice Jing Kun Ip, et al.
Pageof 17

Showing results (101-110 of 168) with videos related to

Sort By:
Pageof 17
Rheumatology (Oxford, England)|January 20, 2025
Distinct genetic risk loci between biopsy-proven renal and non-renal lupus: a 10-year longitudinal cohortShirley Cw Chan, Yao Lei, Desmond Yh Yap, et al.
NPJ Genomic Medicine|August 16, 2018
Exome sequencing for paediatric-onset diseases: impact of the extensive involvement of medical geneticists in the diagnostic odysseyChristopher Cy Mak, Gordon Kc Leung, Gary Tk Mok, et al.
Journal of Autoimmunity|August 3, 2016
Identification of the long noncoding RNA NEAT1 as a novel inflammatory regulator acting through MAPK pathway in human lupusFeifei Zhang, Lingling Wu, Jie Qian, et al.
Lupus Science & Medicine|March 8, 2024
Association of genetic variation on X chromosome with systemic lupus erythematosus in both Thai and Chinese populationsPattarin Tangtanatakul, Yao Lei, Krisana Jaiwan, et al.
Frontiers in Genetics|July 29, 2020
Independent Replication on Genome-Wide Association Study Signals Identifies <i>IRF3</i> as a Novel Locus for Systemic Lupus ErythematosusFeixia Zhang, Yong-Fei Wang, Yan Zhang, et al.
Human Molecular Genetics|February 21, 2020
Genome-wide assessment of genetic risk for systemic lupus erythematosus and disease severityLingyan Chen, Yong-Fei Wang, Lu Liu, et al.
Scientific Reports|November 3, 2016
Novel identified associations of RGS1 and RASGRP1 variants in IgA NephropathyXu-Jie Zhou, Swapan K Nath, Yuan-Yuan Qi, et al.
Arthritis Research & Therapy|May 5, 2018
Meta-analysis of GWAS on both Chinese and European populations identifies GPR173 as a novel X chromosome susceptibility gene for SLEHuoru Zhang, Yan Zhang, Yong-Fei Wang, et al.
Nucleic Acids Research|March 17, 2018
A novel transcript isoform of STING that sequesters cGAMP and dominantly inhibits innate nucleic acid sensingPei-Hui Wang, Sin-Yee Fung, Wei-Wei Gao, et al.
Molecular Autism|January 4, 2018
Identification of mutations in the PI3K-AKT-mTOR signalling pathway in patients with macrocephaly and developmental delay and/or autismKit San Yeung, Winnie Wan Yee Tso, Janice Jing Kun Ip, et al.
Pageof 17